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1.
Clin Exp Immunol ; 141(2): 298-306, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15996194

ABSTRACT

Recognition of repeat CpG motifs, which are common in bacterial, but not in mammalian, DNA, through Toll-like receptor (TLR)9 is an integral part of the innate immune system. As the role of TLR9 in the human gut is unknown, we determined the spectrum of TLR9 expression in normal and inflamed colon and examined how epithelial cells respond to specific TLR9 ligand stimulation. TLR9 expression was measured in human colonic mucosal biopsies, freshly isolated human colonic epithelial cells and HT-29 cells by reverse transcriptase-polymerase chain reaction or Western blotting. Colonic epithelial cell cultures were stimulated with a synthetic CpG-oligodeoxynucleotide (ODN), exhibiting strong immunostimulatory effects in B cells. Interleukin (IL)-8 secretion was determined by enzyme-linked immunosorbent assay, nuclear factor-kappaB (NF-kB) activity by electrophoretic mobility shift assay and IkB phosphorylation by Western blotting. TLR9 mRNA was equally expressed in colonic mucosa from controls (n = 6) and patients with ulcerative colitis or Crohn's disease disease (n = 13). HT-29 cells expressed TLR9 mRNA and protein and responded to CpG-ODN (P < 0.01), but not to non-CpG-ODN stimulation, by secreting IL-8, apparently in the absence of NF-kB activation. Primary epithelial cells isolated from normal human colon expressed TLR9 mRNA, but were completely unresponsive to CpG-ODN stimulation in vitro. In conclusion, differentiated human colonic epithelial cells are unresponsive to TLR9 ligand stimulation in vitro despite spontaneous TLR9 gene expression. This suggests that the human epithelium is able to avoid inappropriate immune responses to luminal bacterial products through modulation of the TLR9 pathway.


Subject(s)
Intestinal Mucosa/metabolism , Membrane Glycoproteins/metabolism , Oligodeoxyribonucleotides/pharmacology , Receptors, Cell Surface/metabolism , Adult , Aged , Aged, 80 and over , Blotting, Western , Cell Line, Transformed , Cells, Cultured , Colitis, Ulcerative/metabolism , Colon/immunology , Colon/metabolism , Crohn Disease/metabolism , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Female , Gene Expression Regulation/drug effects , Humans , I-kappa B Proteins/metabolism , Interleukin-8/metabolism , Intestinal Mucosa/drug effects , Intestinal Mucosa/immunology , Male , Membrane Glycoproteins/genetics , Middle Aged , NF-kappa B/metabolism , RNA, Messenger/genetics , Receptors, Cell Surface/genetics , Reverse Transcriptase Polymerase Chain Reaction , Toll-Like Receptor 9 , Toll-Like Receptors
2.
Bioinformatics ; 19(17): 2319-20, 2003 Nov 22.
Article in English | MEDLINE | ID: mdl-14630664

ABSTRACT

UNLABELLED: A wealth of bioinformatics tools and databases has been created over the last decade and most are freely available to the general public. However, these valuable resources live a shadow existence compared to experimental results and methods that are widely published in journals and relatively easily found through publication databases such as PubMed. For the general scientist as well as bioinformaticists, these tools can deliver great value to the design and analysis of biological and medical experiments, but there is no inventory presenting an up-to-date and easily searchable index of all these resources. To remedy this, the BioWareDB search engine has been created. BioWareDB is an extensive and current catalog of software and databases of relevance to researchers in the fields of biology and medicine, and presently consists of 2800 validated entries. AVAILABILITY: BioWareDB is freely available over the Internet at http://www.biowaredb.org/


Subject(s)
Abstracting and Indexing/methods , Biomedical Research/methods , Catalogs as Topic , Database Management Systems , Databases, Factual , Information Storage and Retrieval/methods , Internet , Software
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